LnK Spinal Fixation System

FDA UDI

Class II (US FDA UDI)

by L&K Biomed Co. , Ltd.

Identity

Trade Name: LnK Spinal Fixation System FDA UDI
Generic Name: Bone-screw internal spinal fixation system rod FDA UDI
Device Name: L&K Biomed Rod, Curved, CoCrMo 6.35x135mm 1EA FDA UDI
Model / Reference: 1074-63135 FDA UDI
Description: L&K Biomed Rod, Curved, CoCrMo 6.35x135mm 1EA FDA UDI

Identifiers

Catalog Number: 1074-63135 FDA UDI
Primary DI / UDI-DI: 08806189856283 FDA UDI
FDA Product Code: NKB FDA UDI
MNI FDA UDI
MNH FDA UDI
KWQ FDA UDI
KWP FDA UDI
GMDN Term: Bone-screw internal spinal fixation system rod FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3060 FDA UDI
888.3050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone-screw internal spinal fixation system rod

LnK Spinal Fixation System by L&K Biomed Co. , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: L&K Biomed Co. , Ltd.

Sources (1)

FDA UDI ba334d18-e2ad-4cc6-bc51-7ccb5df24f28 34 fields · synced May 30, 2026